| Distance: | Resume alert | Resumes 131 - 140 of 638 |
Materials Control associate II
Silver Spring, MD
... Will participate in regulatory (FDA, EMEA) and client audits/inspections of Catalent and the facility. Works closely with QA to quarantine and release all GMP materials in a timely manner. Participation in the organization and cleanliness of the ... - 2024 Jul 30
... Will participate in regulatory (FDA, EMEA) and client audits/inspections of Catalent and the facility. Works closely with QA to quarantine and release all GMP materials in a timely manner. Participation in the organization and cleanliness of the ... - 2024 Jul 30
Web Developer Front-End
Annandale, VA
... ad campaigns, corporate email, and iPad-based Interactive Sales and Marketing Aids • Ensured all projects passed rigorous FDA compliance in a timely manner • Wrote productivity-boosting Bash scripts to automate tedious workflow and ensure accuracy ... - 2024 Jul 27
... ad campaigns, corporate email, and iPad-based Interactive Sales and Marketing Aids • Ensured all projects passed rigorous FDA compliance in a timely manner • Wrote productivity-boosting Bash scripts to automate tedious workflow and ensure accuracy ... - 2024 Jul 27
Member Services Process Improvement
Washington, DC
... Food and Drug Law Institute Washington, DC Manager, Customer Service 1997-1998 FDLI is a non-partisan, non-lobbying organization dedicated to educating the FDA-regulated industries about food and drug law. Reported to Executive Vice President. ... - 2024 Jul 26
... Food and Drug Law Institute Washington, DC Manager, Customer Service 1997-1998 FDLI is a non-partisan, non-lobbying organization dedicated to educating the FDA-regulated industries about food and drug law. Reported to Executive Vice President. ... - 2024 Jul 26
Clinical Research Data Management
Alexandria, VA
... applied deep knowledge of all phases of clinical trial research to ensure compliance in data collection, handling, and processing in compliance with regulatory standards and FDA guidelines, including ISO, FDA, GCP/ICH, SDTM, and 21 CFR Part 1. • ... - 2024 Jul 26
... applied deep knowledge of all phases of clinical trial research to ensure compliance in data collection, handling, and processing in compliance with regulatory standards and FDA guidelines, including ISO, FDA, GCP/ICH, SDTM, and 21 CFR Part 1. • ... - 2024 Jul 26
It Infrastructure Security Analyst
Potomac, MD
... Worked with eCTD is the standard format for submitting applications, amendments, supplements, and reports to FDA’s Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER). Worked on flow designer is a ... - 2024 Jul 15
... Worked with eCTD is the standard format for submitting applications, amendments, supplements, and reports to FDA’s Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER). Worked on flow designer is a ... - 2024 Jul 15
R D Engineer
Silver Spring, MD
... • Established appropriate test protocols for product verifications and validations following GMP, FDA, ISO operational procedures, ISO 9001, ISO 13485, and ISO 14971. • Contributed to technical support and the creation of quality protocols, Engineer ... - 2024 Jul 07
... • Established appropriate test protocols for product verifications and validations following GMP, FDA, ISO operational procedures, ISO 9001, ISO 13485, and ISO 14971. • Contributed to technical support and the creation of quality protocols, Engineer ... - 2024 Jul 07
Clinical Research Patient Care
Washington, DC
... Clinical Research Training: Clinical Research Fastrack Mar 2023 Clinical Research Training covering Core Competencies to include: ●ICH GCP E6 R (2) ●FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 ●Data Management ●Informed Consent ... - 2024 Jul 04
... Clinical Research Training: Clinical Research Fastrack Mar 2023 Clinical Research Training covering Core Competencies to include: ●ICH GCP E6 R (2) ●FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 ●Data Management ●Informed Consent ... - 2024 Jul 04
Public Health Research Scientist
Washington, DC
... PROFESSIONAL CERTIFICATIONS FDA ICH E6 (R2) GDP- ALCOA-C principles & trial protocols & others: Clinical Research Fastrack - TransCelerate Approved (2023) PATIENTS Professors Academy- University of Maryland School of Pharmacy (2023) Chemicals and ... - 2024 Jun 25
... PROFESSIONAL CERTIFICATIONS FDA ICH E6 (R2) GDP- ALCOA-C principles & trial protocols & others: Clinical Research Fastrack - TransCelerate Approved (2023) PATIENTS Professors Academy- University of Maryland School of Pharmacy (2023) Chemicals and ... - 2024 Jun 25
plant site manager
Reston, VA
... MI 1998 – 1999 Essential oils, Flavors and menthol manufacturing, FDA products and packaging https://www.wildflavors.com/NA-EN/products/mint-oils-extracts/ Responsible for $ 125 Million P&L & Global Supply Chain management, OUTSOURCING--RM Set $50 ... - 2024 Jun 17
... MI 1998 – 1999 Essential oils, Flavors and menthol manufacturing, FDA products and packaging https://www.wildflavors.com/NA-EN/products/mint-oils-extracts/ Responsible for $ 125 Million P&L & Global Supply Chain management, OUTSOURCING--RM Set $50 ... - 2024 Jun 17
Medical Device Machine Learning
McLean, VA
... and analyzed FDA and IP issues Submitted two invention disclosures and worked closely with Center for Technology Transfer team for patenting RESEARCH PROJECTS Classification of Bladder Tissues with Diagnostic Biomarkers Extracted from Multimodal ... - 2024 Jun 15
... and analyzed FDA and IP issues Submitted two invention disclosures and worked closely with Center for Technology Transfer team for patenting RESEARCH PROJECTS Classification of Bladder Tissues with Diagnostic Biomarkers Extracted from Multimodal ... - 2024 Jun 15